منابع مشابه
Chronic Acquired Hemolytic Anemia Associated with Hemoglobinuria and Raynaud’s Phenomena
idiopathic acquired hemolytic atsemia, Group II, hemolytic atsemia followitsg irus pmseumomsia and Group III, chrotsic hemolytic atsemia with hemoglohitsuria and Raynaud’s phemsomena. A detailed accoumst. of the climsical aspects of tise three patients of Group III was published by Ferrimams, Dacie, Keele amid Fullerton2 who also made an amsalysis of msine similar cases reported in the literatu...
متن کاملChronic acquired hemolytic anemia associated with hemoglobinuria and Raynaud's phenomena.
idiopathic acquired hemolytic atsemia, Group II, hemolytic atsemia followitsg irus pmseumomsia and Group III, chrotsic hemolytic atsemia with hemoglohitsuria and Raynaud’s phemsomena. A detailed accoumst. of the climsical aspects of tise three patients of Group III was published by Ferrimams, Dacie, Keele amid Fullerton2 who also made an amsalysis of msine similar cases reported in the literatu...
متن کاملAutohemagglutinins and hemolysins with hemoglobinuria and acute hemolytic anemia, in an illness resembling infectious mononucleosis.
CUTE acquired hemolytic anemia is uncommon, but dramatic in its clinical picture and often disastrous in its outcome. In 1940, Dameshek and Schwartz’ assembled about ioo cases reported in the literature since 1907, in which no definite etiology was evident. In addition, as cited by these authors, cases have been reported in which the anemia developed in association with definite or probable eti...
متن کاملTwo Cases of Chronic Hemolytic Anemia Associated with Spherocytosis
Two cases of hemolytic anemia with spherocytosis were investigated. lnspite of chronic hemolysis tl::crc was no radiological changes in flat bones. Management and entity of spherocytosis is discussed m detail in this paper.
متن کاملThymoma with Autoimmune Hemolytic Anemia
A 38-year-old Japanese male was referred to our hospital with abnormal chest X-ray results and severe Coombs-positive hemolytic anemia. He was diagnosed with a stage IV, WHO type A thymoma and was treated with oral prednisolone (1 mg/kg/day) and subsequent chemotherapy. After chemotherapy, the patient underwent surgical resection of the thymoma. Hemolysis rapidly disappeared and did not return ...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: American Journal of Clinical Pathology
سال: 1948
ISSN: 0002-9173,1943-7722
DOI: 10.1093/ajcp/18.10.829